Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9383929
rs9383929
6 151590737 intron variant T/A;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9479055
rs9479055
6 151526832 intron variant C/A snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9479068
rs9479068
6 151551313 intron variant G/T snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9479072
rs9479072
6 151569654 intron variant C/T snv 0.43
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9479075
rs9479075
6 151575100 intron variant G/A snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1038304
rs1038304
0.882 0.160 6 151612040 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs6929137
rs6929137
0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2009
dbSNP: rs1023940
rs1023940
6 151611643 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs3734804
rs3734804
6 151618046 missense variant G/A snv 0.49 0.57
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs6932260
rs6932260
6 151618425 3 prime UTR variant T/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs6932603
rs6932603
6 151618635 3 prime UTR variant T/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1007738
rs1007738
11 46827809 intron variant G/A snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs6469804
rs6469804
8 119032590 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs6993813
rs6993813
1.000 0.080 8 119039999 intron variant T/C snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs1564860
rs1564860
8 118963431 intergenic variant C/T snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs6469792
rs6469792
8 118996132 intron variant T/C snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs10086835
rs10086835
8 119027942 intron variant C/T snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10091277
rs10091277
8 119022148 intron variant A/G snv 0.53
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10098408
rs10098408
8 119027482 intron variant T/C snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10505348
rs10505348
8 118960457 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10505351
rs10505351
8 119021759 intron variant C/T snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10955919
rs10955919
8 119008679 intron variant C/G snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10955924
rs10955924
8 119041104 intron variant C/A snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs11992136
rs11992136
8 118991488 upstream gene variant C/G snv 0.61
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs11995824
rs11995824
8 119000461 intron variant C/G snv 0.65
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2018